Genome-wide identification and characterization of perirenal adipose tissue microRNAs in rabbits fed a high-fat diet

Biosci Rep. 2021 Apr 30;41(4):BSR20204297. doi: 10.1042/BSR20204297.

Abstract

MicroRNAs (miRNAs) are a class of endogenous single-stranded RNA molecules that play an important role in gene regulation in animals by pairing with target gene mRNA. Extensive evidence shows that miRNAs are key players in metabolic regulation and the development of obesity. However, the systemic understanding of miRNAs in the adipogenesis of obese rabbits need further investigation. Here, seven small RNA libraries from rabbits fed either a standard normal diet (SND; n=3) or high-fat diet (HFD; n=4) were constructed and sequenced. Differentially expressed (DE) miRNAs were identified using the edgeR data analysis package from R. Software miRanda and RNAhybrid were used to predict the target genes of miRNAs. To further explore the functions of DE miRNAs, Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis were performed. A total of 81449996 clean reads were obtained from the seven libraries, of which, 52 known DE miRNAs (24 up-regulated, 28 down-regulated) and 31 novel DE miRNAs (14 up-regulated, 17 down-regulated) were identified. GO enrichment analysis revealed that the DE miRNAs target genes were involved in intermediate filament cytoskeleton organization, intermediate filament-based process, and α-tubulin binding. DE miRNAs were involved in p53 signaling, linoleic acid metabolism, and other adipogenesis-related KEGG pathways. Our study further elucidates the possible functions of DE miRNAs in rabbit adipogenesis, contributing to the understanding of rabbit obesity.

Keywords: Adipogenesis; High-fat diet; MiRNAs; Rabbits.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actin Cytoskeleton / metabolism
  • Animals
  • Diet, High-Fat
  • Female
  • Intra-Abdominal Fat / metabolism*
  • Linoleic Acid / metabolism
  • MicroRNAs / genetics
  • MicroRNAs / metabolism*
  • Obesity / etiology
  • Obesity / metabolism*
  • Rabbits
  • Tumor Suppressor Protein p53 / metabolism

Substances

  • MicroRNAs
  • Tumor Suppressor Protein p53
  • Linoleic Acid